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Variant

FDA UDI

Class I (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name
VARIANT FDA UDI
Generic Name
Ophthalmic surgical device handling forceps, reusable FDA UDI
Device Name
Blade #2, 20mm x 200mm FDA UDI
Model / Reference
SPO-115-220 FDA UDI
Description
Blade #2, 20mm x 200mm FDA UDI

Identifiers

Primary DI / UDI-DI
B030SPO1152200 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Ophthalmic surgical device handling forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical device handling forceps, reusable

Variant by Camber Spine Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical device handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Camber Spine Technologies

Sources (1)

  • FDA UDI cbab22d0-1561-4deb-b0ea-416db19793f6 34 fields · synced Jun 6, 2026